Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers
Triblock copolymers of polystyrene (PS) and a polyolefin (PO), e.g., PS-block-poly(ethylene-co-1-butene)-block-PS (SEBS), are attractive materials for use as thermoplastic elastomers and are produced commercially by a two-step process that involves the costly hydrogenation of PS-block-polybutadiene-...
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doaj-7e226a8a3c0747fea92760864a3ae43d2020-11-25T00:53:14ZengMDPI AGPolymers2073-43602017-10-0191048110.3390/polym9100481polym9100481Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block CopolymersChung Sol Kim0Seung Soo Park1Sung Dong Kim2Su Jin Kwon3Jun Won Baek4Bun Yeoul Lee5Department of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaDepartment of Molecular Science and Technology, Ajou University, Suwon 443-749, KoreaTriblock copolymers of polystyrene (PS) and a polyolefin (PO), e.g., PS-block-poly(ethylene-co-1-butene)-block-PS (SEBS), are attractive materials for use as thermoplastic elastomers and are produced commercially by a two-step process that involves the costly hydrogenation of PS-block-polybutadiene-block-PS. We herein report a one-pot strategy for attaching PS chains to both ends of PO chains to construct PS-block-PO-block-PS directly from olefin and styrene monomers. Dialkylzinc compound containing styrene moieties ((CH2=CHC6H4CH2CH2)2Zn) was prepared, from which poly(ethylene-co-propylene) chains were grown via “coordinative chain transfer polymerization” using the pyridylaminohafnium catalyst to afford di-end functional PO chains functionalized with styrene and Zn moieties. Subsequently, PS chains were attached at both ends of the PO chains by introduction of styrene monomers in addition to the anionic initiator Me3SiCH2Li·(pmdeta) (pmdeta = pentamethyldiethylenetriamine). We found that the fraction of the extracted PS homopolymer was low (~20%) and that molecular weights were evidently increased after the styrene polymerization (ΔMn = 27–54 kDa). Transmission electron microscopy showed spherical and wormlike PS domains measuring several tens of nm segregated within the PO matrix. Optimal tensile properties were observed for the sample containing a propylene mole fraction of 0.25 and a styrene content of 33%. Finally, in the cyclic tensile test, the prepared copolymers exhibited thermoplastic elastomeric properties with no breakage up over 10 cycles, which is comparable to the behavior of commercial-grade SEBS.https://www.mdpi.com/2073-4360/9/10/481coordinative chain transfer polymerizationdi-end-functional polyolefinblock copolymerthermoplastic elastomer |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chung Sol Kim Seung Soo Park Sung Dong Kim Su Jin Kwon Jun Won Baek Bun Yeoul Lee |
spellingShingle |
Chung Sol Kim Seung Soo Park Sung Dong Kim Su Jin Kwon Jun Won Baek Bun Yeoul Lee Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers Polymers coordinative chain transfer polymerization di-end-functional polyolefin block copolymer thermoplastic elastomer |
author_facet |
Chung Sol Kim Seung Soo Park Sung Dong Kim Su Jin Kwon Jun Won Baek Bun Yeoul Lee |
author_sort |
Chung Sol Kim |
title |
Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers |
title_short |
Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers |
title_full |
Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers |
title_fullStr |
Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers |
title_full_unstemmed |
Polystyrene Chain Growth from Di-End-Functional Polyolefins for Polystyrene-Polyolefin-Polystyrene Block Copolymers |
title_sort |
polystyrene chain growth from di-end-functional polyolefins for polystyrene-polyolefin-polystyrene block copolymers |
publisher |
MDPI AG |
series |
Polymers |
issn |
2073-4360 |
publishDate |
2017-10-01 |
description |
Triblock copolymers of polystyrene (PS) and a polyolefin (PO), e.g., PS-block-poly(ethylene-co-1-butene)-block-PS (SEBS), are attractive materials for use as thermoplastic elastomers and are produced commercially by a two-step process that involves the costly hydrogenation of PS-block-polybutadiene-block-PS. We herein report a one-pot strategy for attaching PS chains to both ends of PO chains to construct PS-block-PO-block-PS directly from olefin and styrene monomers. Dialkylzinc compound containing styrene moieties ((CH2=CHC6H4CH2CH2)2Zn) was prepared, from which poly(ethylene-co-propylene) chains were grown via “coordinative chain transfer polymerization” using the pyridylaminohafnium catalyst to afford di-end functional PO chains functionalized with styrene and Zn moieties. Subsequently, PS chains were attached at both ends of the PO chains by introduction of styrene monomers in addition to the anionic initiator Me3SiCH2Li·(pmdeta) (pmdeta = pentamethyldiethylenetriamine). We found that the fraction of the extracted PS homopolymer was low (~20%) and that molecular weights were evidently increased after the styrene polymerization (ΔMn = 27–54 kDa). Transmission electron microscopy showed spherical and wormlike PS domains measuring several tens of nm segregated within the PO matrix. Optimal tensile properties were observed for the sample containing a propylene mole fraction of 0.25 and a styrene content of 33%. Finally, in the cyclic tensile test, the prepared copolymers exhibited thermoplastic elastomeric properties with no breakage up over 10 cycles, which is comparable to the behavior of commercial-grade SEBS. |
topic |
coordinative chain transfer polymerization di-end-functional polyolefin block copolymer thermoplastic elastomer |
url |
https://www.mdpi.com/2073-4360/9/10/481 |
work_keys_str_mv |
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